A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028256



Internal ID19117474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9901840..9924385hg38UCSC Ensembl
Innerchr5:9901952..9924497hg19UCSC Ensembl
Innerchr5:9954952..9977497hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3822546
hg1922546
hg1822546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5567n100
Supporting Variantsnssv3638134, nssv3638133, nssv3638146, nssv3748652, nssv3638136, nssv3638138, nssv3748661, nssv3748662, nssv3748660, nssv3748654, nssv3638144, nssv3748659, nssv3748664, nssv3748651, nssv3748655, nssv3748656, nssv3748665, nssv3638141, nssv3748657, nssv3638135, nssv3638145, nssv3638140, nssv3638143, nssv3748658, nssv3748663, nssv3638142, nssv3638137, nssv3748666, nssv3748653, nssv3638139
Samples
Known GenesLOC285692
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028256
Frequency
Sample Size11257
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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